Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321121010 | Autosomal dominant macrothrombocytopenia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321122015 | Autosomal dominant macrothrombocytopenia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402393019 | A rare isolated constitutional thrombocytopenia characterized by abnormally large platelets. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402394013 | A rare isolated constitutional thrombocytopenia characterised by abnormally large platelets. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3321121010 | Autosomal dominant macrothrombocytopenia (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321121010 | Autosomal dominant macrothrombocytopenia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321122015 | Autosomal dominant macrothrombocytopenia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321122015 | Autosomal dominant macrothrombocytopenia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321123013 | This syndrome has characteristics of congenital thrombocytopenia associated with the presence of large platelets. To date less than 10 cases are reported. The syndrome is caused by mutations in the integrin, beta 3 ITGB3, tubulin, beta-1TUBB1 and actinin, alpha1 ACTN1 genes. These mutations lead to abnormal proplatelets and thrombocytopenia. Transmission is autosomal dominant. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402393019 | A rare isolated constitutional thrombocytopenia characterized by abnormally large platelets. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402394013 | A rare isolated constitutional thrombocytopenia characterised by abnormally large platelets. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3385371001000119 | Makrothrombozytopenie, autosomal-dominante | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1006201000172116 | macrothrombocytopénie autosomique dominant | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1006201000172116 | macrothrombocytopénie autosomique dominant | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3385371001000119 | Makrothrombozytopenie, autosomal-dominante | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)